Sr. Process Engineer/Project Manager in Westborough, Massachusetts at Pall

Date Posted: 7/5/2018

Job Snapshot

Job Description

Job ID: LIF003681

About Us

Pall Corporation is a global leader in high-tech filtration, separation, and purification, serving the diverse needs of customers across the broad spectrum of life sciences and industry.



Pall Life Sciences provides cutting-edge products and services to meet the demanding needs of customers discovering, developing and producing biotech drugs, vaccines, cell therapies and classic pharmaceuticals. Pall offers advanced medical technologies, which are often a patient’s last line of defense from dangerous pathogens. Pall’s food and beverage products provide critical protection from contaminants during various manufacturing steps.



Pall Industrial serves a diverse range of customers in the microelectronics, aerospace, fuels, petrochemical, chemical, automotive, and power generation industries. Pall is a key supplier to the innovative and demanding semiconductor and consumer electronics industries, and provides filtration products used in critical applications on commercial and military aerospace vehicles. Pall products are key to the reliability of industrial equipment. Pall’s engineered solutions help municipal and industrial customers address mounting water quality, scarcity and demand issues, and help energy companies maximize production and develop commercially successful next generation fuels.



Headquartered in Port Washington, New York, Pall has offices and plants throughout the world.



To learn more about Pall, please visit www.pall.com/green.



Description

Senior Process Engineer/Project Manager will lead a team of Process Engineers/Project Managers in the design of systems for both small and large Biotechnology companies. Sr. PE/PM will possess strong process knowledge and mechanical design including size equipment, valves and pumps.  Sr. PE/PM will also interact with customers on applications to select, develop and size out equipment.





Primary Responsibilities:


Define technical process (technology selection, sizing, design testing etc.) working with the customer on requested equipment.


•Provide technical proposal and costing for the proposed solution.


•Own the project execution and guide a multidisciplinary team from inception through project completion (establish the project plan, coordinate project team activities, report progress.


•Control project scope, schedule and budget relative to the established baseline.


•Elaborate design detail design (including functional specification, define and creation of instrument, valve, apparatuses and fitting lists etc.).


•Ensure design comply with current pharmaceutical standards applicable for the project such as ASME BPE, GAMP, cGMP, ISPE guidelines.


•Work in accordance to our established quality management system.


•Supply all technical documentation in accordance to the specification for the project.


•Execute and coordinate all qualification activities included in the project (pre-Factory Acceptance


•Testing, Factory Acceptance Testing, and Site Acceptance Testing).


•Assist customers in their qualification and validation activities if requested


•Travel up to 20% in North America including Puerto Rico


Job Requirements



Qualifications

Qualifications:


Define technical process (technology selection, sizing, design testing etc.) working with the customer on requested equipment.


•Provide technical proposal and costing for the proposed solution.


•Own the project execution and guide a multidisciplinary team from inception through project completion (establish the project plan, coordinate project team activities, report progress.


•Control project scope, schedule and budget relative to the established baseline.


•Elaborate design detail design (including functional specification, define and creation of instrument, valve, apparatuses and fitting lists etc.).


•Ensure design comply with current pharmaceutical standards applicable for the project such as ASME BPE, GAMP, cGMP, ISPE guidelines.


•Work in accordance to our established quality management system.


•Supply all technical documentation in accordance to the specification for the project.


•Execute and coordinate all qualification activities included in the project (pre-Factory Acceptance


•Testing, Factory Acceptance Testing, and Site Acceptance Testing).


•Assist customers in their qualification and validation activities if requested


•Travel up to 20% in North America including Puerto Rico



Preferred Qualifications:


MSc in Biochemical engineering, Process engineering, Chemical engineering, Mechanical engineering, or equivalent.


The above describes the essential content of and requirements for proficient performance in the position and is not meant to be all-inclusive.




Danaher Corporation Overview

Danaher is a global science & technology innovator committed to helping our customers solve complex challenges and improve quality of life worldwide. Our world class brands are leaders in some of the most demanding and attractive industries, including life sciences, medical diagnostics, dental, environmental and applied solutions. Our globally diverse team of 67,000 associates is united by a common culture and operating system, the Danaher Business System, which serves as our competitive advantage. We generated $18.3B in revenue last year. We are ranked #162 on the Fortune 500 and our stock has outperformed the S&P 500 by more than 1,200% over 20 years.
At Danaher, you can build a career in a way no other company can duplicate. Our brands allow us to offer dynamic careers across multiple industries. We’re innovative, fast-paced, results-oriented, and we win. We need talented people to keep winning. Here you’ll learn how DBS is used to shape strategy, focus execution, align our people, and create value for customers and shareholders. Come join our winning team.